WO1996030540A3 - Substrates for beta-lactamase and uses thereof - Google Patents

Substrates for beta-lactamase and uses thereof Download PDF

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Publication number
WO1996030540A3
WO1996030540A3 PCT/US1996/004059 US9604059W WO9630540A3 WO 1996030540 A3 WO1996030540 A3 WO 1996030540A3 US 9604059 W US9604059 W US 9604059W WO 9630540 A3 WO9630540 A3 WO 9630540A3
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WO
WIPO (PCT)
Prior art keywords
beta
group
lactamase
substrates
chr
Prior art date
Application number
PCT/US1996/004059
Other languages
French (fr)
Other versions
WO1996030540A2 (en
Inventor
Roger Y Tsien
Gregor Zlokarnik
Original Assignee
Univ California
Roger Y Tsien
Gregor Zlokarnik
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to DE69612375T priority Critical patent/DE69612375T2/en
Priority to US08/727,616 priority patent/US6291162B1/en
Priority to AT96912454T priority patent/ATE200287T1/en
Priority to DK99118473T priority patent/DK0982398T3/en
Application filed by Univ California, Roger Y Tsien, Gregor Zlokarnik filed Critical Univ California
Priority to EP96912454A priority patent/EP0817785B1/en
Priority to JP52957396A priority patent/JP3633940B2/en
Priority to DK96912454T priority patent/DK0817785T3/en
Priority to CA002215310A priority patent/CA2215310C/en
Priority to AU55266/96A priority patent/AU723164B2/en
Publication of WO1996030540A2 publication Critical patent/WO1996030540A2/en
Publication of WO1996030540A3 publication Critical patent/WO1996030540A3/en
Priority to US09/481,756 priority patent/US6472205B1/en
Priority to US10/280,482 priority patent/US7157575B2/en
Priority to US11/447,691 priority patent/US20070020715A1/en
Priority to US11/606,642 priority patent/US8071761B2/en

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    • C07D501/00Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/207-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/247-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
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    • C12P17/18Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing at least two hetero rings condensed among themselves or condensed with a common carbocyclic ring system, e.g. rifamycin
    • C12P17/182Heterocyclic compounds containing nitrogen atoms as the only ring heteroatoms in the condensed system
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    • C12Q2334/00O-linked chromogens for determinations of hydrolase enzymes, e.g. glycosidases, phosphatases, esterases
    • GPHYSICS
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    • G01N2333/978Hydrolases (3) acting on carbon to nitrogen bonds other than peptide bonds (3.5)
    • G01N2333/986Hydrolases (3) acting on carbon to nitrogen bonds other than peptide bonds (3.5) acting on amide bonds in cyclic amides (3.5.2), e.g. beta-lactamase (penicillinase, 3.5.2.6), creatinine amidohydrolase (creatininase, EC 3.5.2.10), N-methylhydantoinase (3.5.2.6)
    • GPHYSICS
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    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
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Abstract

Substrates for beta -lactamase of general formula (I) in which one of X and Y is a fluorescent donor moiety and the other is a quencher (which may or may not re-emit); R' is selected from the group consisting of H, lower (i.e. alkyl of 1 to about 5 carbon atoms) and (CH2)nOH, in which n is 0 or an integer from 1 to 5; R" is selected from the group consisting of H, physiologically acceptable metal and ammonium cations, - CHR<2>OCO(CH2)nCH3, -CHR<2>OCOC(CH3)3, acylthiomethyl, acyloxy-alpha-benzyl, delta-butyrolactonyl, methoxycarbonyloxymethyl, phenyl, methylsulphinylmethyl, beta-morpholinoethyl, dialkylaminoethyl, acyloxyalkyl, dialkylaminocarbonyloxymethyl and aliphatic, in which R<2> is selected from the group consisting of H and lower alkyl; A is selected from the group consisting of S, O, SO, SO2 and CH2; and Z' and Z" are linkers for the fluorescent donor and quencher moieties. Methods of assaying beta -lactamase activity and monitoring expression in systems using beta -lactamase as a reporter gene also are disclosed. <IMAGE> <IMAGE>
PCT/US1996/004059 1995-03-20 1996-03-20 Substrates for beta-lactamase and uses thereof WO1996030540A2 (en)

Priority Applications (13)

Application Number Priority Date Filing Date Title
JP52957396A JP3633940B2 (en) 1995-03-20 1996-03-20 Substrate for β-lactamase and use thereof
AT96912454T ATE200287T1 (en) 1995-03-20 1996-03-20 SUBSTRATES FOR BETA-LACTAMASE AND THE USE THEREOF
DK99118473T DK0982398T3 (en) 1995-03-20 1996-03-20 Nucleic acids and uses thereof for the study of beta-lactamase
CA002215310A CA2215310C (en) 1995-03-20 1996-03-20 Substrates for beta-lactamase and uses thereof
EP96912454A EP0817785B1 (en) 1995-03-20 1996-03-20 Substrates for beta-lactamase and uses thereof
US08/727,616 US6291162B1 (en) 1995-03-20 1996-03-20 Cytosolic forms of beta-lactamase and uses thereof
DK96912454T DK0817785T3 (en) 1995-03-20 1996-03-20 Substrates for beta-lactamase and its use
DE69612375T DE69612375T2 (en) 1995-03-20 1996-03-20 SUBSTRATES FOR BETA LACTAMASE AND THEIR USE
AU55266/96A AU723164B2 (en) 1995-03-20 1996-03-20 Substrates for beta-lactamase and uses thereof
US09/481,756 US6472205B1 (en) 1995-03-20 2000-01-11 Cytosolic forms for β-lactamase and uses thereof
US10/280,482 US7157575B2 (en) 1995-03-20 2002-10-24 Substrates for β-lactamase and uses thereof
US11/447,691 US20070020715A1 (en) 1995-03-20 2006-06-05 Novel fluorogenic substrates for beta-lactamase gene expression
US11/606,642 US8071761B2 (en) 1995-03-20 2006-11-29 Substrates for beta-lactamase and uses thereof

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US08/407,544 1995-03-20
US08/407,544 US5741657A (en) 1995-03-20 1995-03-20 Fluorogenic substrates for β-lactamase and methods of use

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US08/407,544 Continuation-In-Part US5741657A (en) 1995-03-20 1995-03-20 Fluorogenic substrates for β-lactamase and methods of use

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US08/727,616 Continuation US6291162B1 (en) 1995-03-20 1996-03-20 Cytosolic forms of beta-lactamase and uses thereof

Publications (2)

Publication Number Publication Date
WO1996030540A2 WO1996030540A2 (en) 1996-10-03
WO1996030540A3 true WO1996030540A3 (en) 1997-01-09

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Application Number Title Priority Date Filing Date
PCT/US1996/004059 WO1996030540A2 (en) 1995-03-20 1996-03-20 Substrates for beta-lactamase and uses thereof

Country Status (13)

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US (5) US5741657A (en)
EP (3) EP0982398B1 (en)
JP (2) JP3633940B2 (en)
CN (2) CN1066731C (en)
AT (3) ATE253632T1 (en)
AU (1) AU723164B2 (en)
CA (1) CA2215310C (en)
DE (2) DE69630622T2 (en)
DK (2) DK0817785T3 (en)
ES (2) ES2209305T3 (en)
MX (1) MX9707213A (en)
PT (1) PT982398E (en)
WO (1) WO1996030540A2 (en)

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